WO1993010167A1 - Compositions de revetement contenant des composants urethanes et epoxy, et articles revetus de ces compositions - Google Patents

Compositions de revetement contenant des composants urethanes et epoxy, et articles revetus de ces compositions Download PDF

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Publication number
WO1993010167A1
WO1993010167A1 PCT/US1992/009941 US9209941W WO9310167A1 WO 1993010167 A1 WO1993010167 A1 WO 1993010167A1 US 9209941 W US9209941 W US 9209941W WO 9310167 A1 WO9310167 A1 WO 9310167A1
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WO
WIPO (PCT)
Prior art keywords
hardener
weight
amine
set forth
epoxy
Prior art date
Application number
PCT/US1992/009941
Other languages
English (en)
Inventor
Bipin C. Pant
Shirish A. Pandit
Hemant A. Naik
Ratanjit S. Sondhe
Original Assignee
Pant Bipin C
Pandit Shirish A
Naik Hemant A
Sondhe Ratanjit S
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pant Bipin C, Pandit Shirish A, Naik Hemant A, Sondhe Ratanjit S filed Critical Pant Bipin C
Priority to EP19920925304 priority Critical patent/EP0603342B1/fr
Priority to DE1992624480 priority patent/DE69224480T2/de
Publication of WO1993010167A1 publication Critical patent/WO1993010167A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/004—Reflecting paints; Signal paints
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D5/00—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
    • B05D5/06—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain multicolour or other optical effects
    • B05D5/061—Special surface effect
    • B05D5/063—Reflective effect
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/50—Multilayers
    • B05D7/52—Two layers
    • B05D7/54—No clear coat specified
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/088—Removal of water or carbon dioxide from the reaction mixture or reaction components
    • C08G18/0885—Removal of water or carbon dioxide from the reaction mixture or reaction components using additives, e.g. absorbing agents
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4266—Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from hydroxycarboxylic acids and/or lactones
    • C08G18/4269—Lactones
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D2503/00—Polyurethanes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D2504/00—Epoxy polymers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/252—Glass or ceramic [i.e., fired or glazed clay, cement, etc.] [porcelain, quartz, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31511—Of epoxy ether
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31511—Of epoxy ether
    • Y10T428/31515—As intermediate layer
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31598—Next to silicon-containing [silicone, cement, etc.] layer
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31605—Next to free metal

Definitions

  • the present invention relates to generally a volatile-free, two-part, epoxy composition, and to generally a volatile-free, two-part, urethane composition, and to an article made therefrom by generally coating the urethane composition on the epoxy composition.
  • U.S. Patent No. 3,136,733 to Ross et al relates to highway marking material adapted for marking pavements of roads, streets, highways, aircraft landing strips, and the like, for defining traffic lanes, pedestrian cross-walks, traffic instructions, and the like.
  • U.S. Patent No. 4,554,214 to Ichinomiya et al relates to a polyurethane type casting coating which is used as labelling materials in labels, stickers, outdoor signs, reflective refractors, light road markings or automobiles.
  • U.S. Patent No. 4,689,268 to Meader, Jr. relates to a concrete surface coated with a cast in place surfacing composition comprising at least three layers, in order from the concrete surface:
  • a first layer comprising:
  • a second layer comprising a bonding agent which improves adhesion between said first and third layers, and;
  • a third layer comprising: (l) 20 to 80 parts by weight of a polyurethane, said polyurethane formed by reacting a polyisocyanate with a polyurethane precursor at a mole ratio of 0.8 to 1.4:1, said polyurethane precursor comprising 15 to 60 parts by weight of a high molecular weight polyol and 2 to 10 parts by weight of a low molecular weight chain stiffener, (2) 20 to 80 parts by weight of a substantially non-volatile extender, and (3) 0 to 20 parts by weight of a volatile solvent.
  • U.S. Patent No. 4,699,814 to Ambrose et al relates to an improved process of preparing color-plus- clear coatings, the improvement comprising an epoxyfunctional polyurethane resin and high solids thermosetting coating compositions prepared therewith.
  • U.S. Patent No. 4,732,790 to Blackburn et al relates to an improved process for preparing color-plusclear coatings, the improvement comprising high solids thermosetting coating compositions comprising hydroxy- functional polyepoxides and anhydrides as effective curing agents therefor. Films of these coating compositions have low volatile organic content (VOC).
  • VOC volatile organic content
  • U.S. Patent No. 4,758,469 to Lange relates to pavement marking comprising ceramic microspheres held by a binder, said microspheres being solid, transparent, non-vitreous, ceramic particles which serve as lens elements in the retro reflective pavement markings.
  • the ceramic microspheres formed by various sol gel techniques are characterized by having at least one metal oxide phase; and an average minimum dimension of up to 125 micrometers.
  • U.S. Patent No. 4,837,069 to Bescup et al relates to a procedure for making AI2O3 spheroids, 600 micrometers in diameter or less, utilizing an AlOOH sol containing 0.25 percent weight percent MgO (in the form of Mg(NO 3 ) 2 ⁇ 6H 2 O) and HNO 3 .
  • the sol is dispersed into droplets in a particle forming fluid (e.g., 2-ethylhexanol) where gelling occurs.
  • the gelled spheroids are collected, dried and pre-fired in air at temperatures less than 1,200°C for up to about 12 hours.
  • the dried and prefired beads are fired in a 2-step process at temperatures of about 1, 850-1, 950°C in the following sequence: a first dry oxygen firing for about ten minutes, followed by a wet hydrogen firing for up to 350 minutes.
  • Reasonably transparent microspheres having crystallites in the range of 5-100 micrometers are obtained with little intergranular porosity, and their density is estimated to be near theoretical.
  • U.S. Patent No. 4,855,185 to Vu et al relates to novel polyurethane formulations especially useful as membranes for the protection of bridge deckings.
  • the polyurethane is prepared by mixing two components, A and B.
  • Component A consists essentially of a low molecular weight polyol, e.g., glycerol; a poly (oxypropylene) triol; and an elastomer.
  • Component B is a special MDI, either a mix of 4,4'- and 2,4'-isomers of diphenyl-methane diisocyanate or a mix of 4,4'-diphenylmethane diisocyanate and its reaction product with a low molecular weight poly(oxypropylene).
  • U.S. Patent No. 4,859,735 to Vu relates to novel polyurethane formulations especially useful as membranes of the protection of bridge deckings.
  • the polyurethane is prepared by mixing two components, A and B.
  • Component A comprises castor oil modified with a ketone-formaldehyde condensate and also preferably contains an elastomer.
  • Component B is a modified MDI, being a mixture of diphenylmethane diisocyanate and its reaction product with a low molecular weight poly(oxyalkylene).
  • U.S. Patent No. 4,877,829 to Vu et al relates to novel polyurethane formulations especially useful as membranes for the protection of bridge deckings.
  • the polyurethane is prepared by mixing two components, A and B.
  • Component A comprises castor oil, a low molecular weight polyol having a molecular weight between 92 and about 200, preferably with an elastomer.
  • Component B is a modified MDI, being either (i) a mix of 4,4'- and 2,4'-isomers of diphenylmethane diisocyanate or (ii) a dephenylmethane diisocyanate and its reaction product with a low molecular weight poly(oxyalkylene).
  • U.S. Patent No. 4,937,127 to Haenggi et al relates to a skid-resistant pavement marking sheet including a top surface and a plurality of skid-resistant ceramic spheroids embedded in and protruding from the surface.
  • the ceramic spheroids are fired from a raw material mixture including 10-97 weight percent mineral particulates, 3-90 weight percent alumina, and at least 1 weight percent binder, at a temperature of about 1300°C, have an outer surface rich in alumina concentration relative to the center of the spheroid, and are resistant to crushing and fracturing.
  • This composition is the reaction product of a epoxy resin, or combination of one or more resins combined with a hardener or a hardener system.
  • the hardener can be an amine hardener such as an aliphatic or aromatic amine hardener, an anhydride hardener or a mercaptan hardener, etc. It is preferable that the hardener is an amine or mercaptan.
  • An amine hardener system comprised of more than one amine hardener is most preferred.
  • the amine hardener system is reacted with the epoxy resin at a equivalent ratio of from about 0.75 to about 1.05, and more preferably at from about 0.9 to about 1.0.
  • the epoxy resin may include a base resin, along with an epoxy resin diluent for the reduction of the viscosity. Further, the resin may contain other additives, such as pigment, thixotropic agents, defoamers, and the like.
  • the amine hardener system comprises one or more amine hardeners which are aliphatic, cycloaliphatic and/or adducts of the same. These hardeners are used at from about 15 to about 40 percent by weight of a first amine hardener (based on the total weight of the amine hardener system), which is an amino alkyl piperazine having from about 1 to about 4 carbon atoms in said alkyl group and an alkyl phenol having from about 1 to about 12 carbon atoms in said alkyl group; from about 45 to about 60 percent by weight of a second amine which is an amine derivative of ethylene, and from about 10 to about 25 percent by weight of a third amine which is an alkyl amino alkyl piperazine when all three hardeners are utilized.
  • the hardener system further includes a catalyst which is preferably a dicarboxylic acid, and a plasticizer such as an aromatic alcohol.
  • the epoxy composition in accordance with this invention has a low tack-free time, appropriate color and resistance to discoloration, appropriate viscosity, adhesion to various substrates including concrete, asphalt, polyurethane and glass beads, and desirable physical properties such as good impact strength compressive and tensile strength and good abrasion resistance. Further, the epoxy provides volatile free or substantially volatile free epoxy for use in road lane markers.
  • the urethane composition is generally a two-part liquid system substantially free of any solvents and contains one or more polyisocyanates and one or more hydroxyl terminated intermediates.
  • the polyisocyanate is a diisocyanate and the equivalent ratio of isocyanate groups to hydroxyl groups of the intermediate is generally from about 0.9 to about 1.5.
  • At least some of the hydroxyl terminated intermediates have a functionality greater than two such as trifunctional compounds so that upon reaction with a diisocyanate, a cured branched or crosslinked polyurethane composition is produced.
  • Moisture scavengers such as latent polyamines can also be utilized along with various catalysts and pigments. Cure generally occurs at ambient temperature.
  • the urethane provides good weathering resistance, good abrasion resistance, good flexibility, good tensile strength and low viscosity.
  • An article is made by coating the urethane composition on the epoxy composition which generally serves as a base layer.
  • the urethane which is generally applied before the epoxy is fully cured and will typically bleed into, intermingle, mechanically bound, etc. with a portion of the epoxy substrate.
  • a composite is formed from the epoxy and the urethane in which the layers are chemically fused and the layers subsequently have substantially no discrete interface but rather the composite has an intermediate section in which one or more compounds of the epoxy resin and/or hardener may join the respective polymeric units of both layers.
  • This can generally be understood to be a form of or at least analogous to chemical bonding, to crosslinking and/or mechanically bonding between the layers.
  • the epoxy layer generally serves as an excellent binder to the substrate as well as to optional reflective additives, i.e., glass beads, whereas the urethane layer has good abrasion resistance and good weatherability and thus can be used as a road lane marker.
  • the combination of the epoxy and the urethane have the additional advantage that since both layers are free from volatiles, such as solvents, the final article is likewise free from volatiles. This is an advantage in the application of the laminate since it eliminates volatiles which could be hazardous to the environment or the workers who apply the laminate to the substrate surface.
  • Articles in the form of a laminate or coated substrates are formed by generally adding a layer of the urethane composition to the epoxy composition.
  • the epoxy composition has good bonding to surfaces such as industrial floors, garage decks, i.e. concrete and steel structures, storage tanks, roads including concrete and asphalt and the like, and hence generally serves as the substrate interface or base layer.
  • the urethane composition has good weatherability resistance as well as generally good abrasion resistance and therefore serves as a good durable top coat.
  • An epoxy composition which has a unique combination of hardeners in a hardener system which are used in a specified ratio in order to achieve the properties of this composition.
  • This epoxy composition is generally a volatile-free system.
  • volatilefree system it is meant that the composition generally contains less than 10 percent by weight of volatile, desirably less than 1 percent by weight, preferably no volatile at all, that is 0 percent, or completely free from volatile which can be released from the composition as a volatile. In the past, such volatiles have often resulted from the use of solvent. Thus, the composition is substantially, or even 100 percent non-solvent at ambient temperature and upon cure is 100 percent solids.
  • the term "volatile-free system” can be understood to be free from organic components which have a boiling point of less than 120°F. This is also known in the art as a 100 percent solids system. This advantage results in a composition which is safer and more environmentally benign than prior art compositions. Despite this advantage, the composition has an appropriate viscosity to permit application such as by spraying.
  • Epoxy compositions are generally formed by the mixing of two components, a part “A” comprising the epoxy resin, and a part “B” comprising the hardener system. The epoxy resin is reacted with a hardener system.
  • the preferred hardener is one or more amine hardeners as will be further discussed in greater detail.
  • Such hardeners include, for example, aliphatic and aromatic amines, amine adducts, cycloaliphaticamines, mercaptans, polyamides, amidoamines, anhydrides and the like.
  • one or more epoxy resin can be used as the base resin with an optional epoxy modifier and other additives.
  • epoxy resins or polymers examples include but are not limited to polyhydric phenol polyether alcohols; glycidyl ethers of novolac resins such as epoxylated phenol-formaldehyde novolac resin; glycidyl ethers of mono-, di-, and trihydric phenols; glycidyl ethers of bisphenols such as diglycidyl ether of tetrabromobisphenol A; glycidyl ethers of polynuclear phenols; epoxy resin made from diphenolic acid; glycidyl ethers of aliphatic polyols such as chlorine-containing aliphatic diepoxy and polyepichlorohydrin; glycidyl esters such as aliphatic diacid glycidyl esters and epoxidized phenolphthalein; glycidyl epoxies containing nitrogen such as glycidyl amides and amide-
  • epoxy resins which can be used include those which are synthesized from mono-epoxies other than epihalohydrins including epoxy resins made from unsaturated monoepoxies such as poly allyl glycidyl ether and glycidyl sorbate dimer; epoxy resins from monoepoxy alcohols; epoxy resins from monoepoxies by ester interchange; epoxy resins from glycidyaldehyde; polyglycidyl compounds containing unsaturation such as allyl-substituted diglycidyl ether of bisphenol A; epoxy-resin adducts of the above; and epoxy resins which are synthesized from olefins and chloroacetyls such as butadiene dioxide, vinylcyclohexane dioxide, epoxidized polybutadiene, and bis(2,3-epoxycyclopentyl) ether.
  • epoxy resins made from unsaturated monoepoxies such as poly allyl
  • the various epoxy resins or polymers which are generally applicable to the present invention as the base epoxy resin have a number average molecular weight of from about 300 to about 5,000, and preferably from about 320 to about 390.
  • the various epoxy polymers useful for the basic epoxy resin generally are difunctional, that is, they have two epoxide groups typically at the terminal portions thereof.
  • a highly preferred base epoxy resin is diglycidyl ether of bisphenol A (DGEBA) which has the following formula:
  • n is an integer from 0 to 18, desirably from 0.05 to 3, and preferably from 0.1 to 2.
  • the base epoxy resin useful for the present invention comprises a bisphenol A type resin, or a blend of bisphenol A resin and epichlorohydrin having a weight per epoxide ranging from about 175 to about 200, and more preferably from about 180 to about 195.
  • the resin has a viscosity at 77°C of from about 6,000 centipoise to about 18,000 centipoises, and more preferably from about 11,000 centipoises to about 16,000 centipoises and most preferably from about 11,000 to about 14,000 centipoises.
  • the resin should have a color APHA of from about 0 to about 200.
  • the epoxy resin can be used with a modifier such as for example a diluent.
  • a modifier such as for example a diluent.
  • these diluents should have an epoxide equivalent weight range of 120- 325.
  • an alkyl glycidyl ether as the diluent with a suitable range being from 2 to 20 carbon atoms in the alkyl portion. More preferably, the alkyl portion contains 3 to 10 carbon atoms, with butylglycidyl ether being most preferred.
  • the diluent may be a diepoxide such as butyldiglycidyl ether.
  • cresyl diglycidyl ether having a weight equivalence of from about 160 to about 210, and more preferably from about 170 to about 195.
  • epoxide fractions of C 2 to C 20 are useful with two specific fractions being in the range of C 8 to C 10 and in the range of C 12 to C 14 could be used.
  • 2-ethylhexylglycidyl ether could be used.
  • butylglycidyl ether it preferably has a weight per epoxide equivalence of from about 120 to about 220, and more preferably from about 130 to about 260.
  • the diluent is used in an amount sufficient to lower the viscosity of the epoxy resin to an appropriate number and will therefore of course depend upon the base resin used.
  • a desired viscosity range for spray applications such as used in the present invention is from about 2,000 to about 15,000 centipoises at 77°F, and more particularly from about 3,000 to about 12,000 centipoises, and most desirably from about 4,000 to 5,000.
  • a preferred amount of the diluent is from about 5 to about 15; preferably from about 8 to about 12; and most preferably from about 6 to about 10 parts by weight per 100 parts by weight of the epoxy base resin.
  • the amount of the diluent added will also depend upon the amount appropriate for the addition of the pigmentation.
  • additives which can be used in the resin system include, for example, pigment.
  • the pigment may be used, added in a desired amount, in a desired color such as for example 10 to 50; preferably 20 to 45 parts by weight per 100 parts by weight of the epoxy resins.
  • a white pigment may be used which can include, for example, titanium dioxide, or a yellow pigment might be used which might include lead chromate.
  • the epoxy can be clear, such as for a clear primer.
  • a thixotropic agent such as amorphous fumed silica, a defoamer, heat and light stabilizers, wetting and dispersing agents, antioxidants, and the like.
  • a hardener system is combined with the epoxy resin in order to produce the resultant epoxy composition.
  • the hardener system utilizes one or more hardeners which could be an amine, an amidoamine, an anhydride or a mercaptan hardener.
  • suitable mercaptans include generally mercaptan terminated polysulfides, such as LP32 and LP3 sold by Morton Thiokol, and Capcure 3800 and Capcure WR6 sold by Henkel. It is preferable that the hardener is one or more amine hardeners which is either aromatic or aliphatic.
  • Suitable aromatic hardeners include methylene dianaline, diaminodiphenylsulphone, aromatic polyamine adducts based on methylenedianiline, modified aromatic adducts based on methylenedianiline and modified methylene dianiline, and m-phenylendiamine, its adducts and derivatives and polyamines, while aliphatic hardeners include alkyl and heterocyclic amines, and their adducts and derivatives.
  • the hardener system preferably includes more than one hardener composition in a more preferred embodiment includes at least three compositions.
  • the system when the system includes a two component system, the system may be 10 to 90 percent by weight of a first hardener and 10 to 90 percent by weight of a second hardener based on the total weight of both hardeners.
  • the system has three or more hardeners, the system has 5 to 90 percent of a first hardener, 5 to 90 percent of a second hardener, and from 5 to 90 percent of a third hardener.
  • these amine hardeners are predominately, if not exclusively, aliphatic.
  • the amine hardeners are used in an amount so that the gram equivalent ratio of the amine functionality to the epoxide functionality of the epoxy system is from about 0.75 to about 1.05, and more preferably from about 0.9 to about 1.0.
  • three amine hardeners are used in combination in the hardener system.
  • these hardeners are at least substantially aliphatic amines since aromatic amines tend to discolor.
  • the first hardener amine (a) is a combination of an alkylphenol and a aliphatic amine which is an amino-alkyl cyclodiamine having the general formula
  • R 1 is an alkyl having 1 to 20 carbon atoms, and preferably 1 to 8 carbon atoms; and R 2 and R 3 , independently, form a heterocyclic alkyl each having 1 to 15 carbon atoms, and preferably 1 to 8 carbon atoms, and R 4 is hydrogen or R 5 NH 2 or R 6 NHR 7 , where R 5 is alkyl C 1 and C 10 and preferably C 1 to C 3 , and R 6 is alkyl C 1 to C 10 and preferably C 1 to C 3 , and R 7 is alkyl C 1 to C 10 and preferably C 1 to C 3 .
  • An example of a preferred cycloamine is amino ethyl piperazine or bis-amino propyl piperazine.
  • This aliphatic amine is activated or modified, meaning that it is combined with an alkyl phenol having a 1 to 15 carbon alkyl, and preferably a 1 to 9 carbon alkyl, such as nonyl phenol.
  • the combination may be an amine adduct.
  • the second amine hardener (b) is again a combination of an aliphatic amine with a phenol.
  • the aliphatic amine could be an amine adduct.
  • the amine is a poly generic amine having the general formula
  • R 8 is (CH 2 ) n , where n is 1 or 2 to 30 and preferably about 2 to 12, and x is 1 to 10, preferably about 1 to 4.
  • Preferred amines are diethylene triamine, methylenetetramine, diethylenepropylamine, tetraethylenepentaamine, and particularly preferred amines are diethylene triamine and triethylene tetramine.
  • the phenol may include bisphenol A or bisphenol F and is preferably is bisphenol A. Again, the combination may result in an amine adduct. A commercial example of this is Versamine 912, sold by Henkel.
  • the third amine hardener (c) is preferably an alkyl amino alkyl cyclodiamine having the general formula
  • R 9 is an alkyl having from about 1 to about 15 carbon atoms, preferably about 1 to about 10, most preferably nonyl;
  • R 10 is an alkyl having from about 1 to about 15; preferably from about 1 to about 8 (e.g. ethyl) and R 11 and R 12 together with the two amine functionalities form a heterocyclic alkyl where R 11 and R 12 , independently, each have from about 1 to about 15; and preferably from 1 to about 4 carbon atoms, and where R 13 is hydrogen, or R 14 H 2 or R 15 NHR 16 , where R 14 is alkyl C 1 to C 10 , and preferably C 1 to C 3 , and R 15 is alkyl C 1 to
  • R16 is alkyl C 1 to C 10 , and preferably C 1 to C 3 .
  • Specific examples include nonylaminoethylpiperazine and bis-aminopropylpiperazine.
  • the preferred amine hardeners are used in combination where, by weight, the first amine hardener (a) is from about 15 to about 40 percent; preferably from about 27 to about 37 percent; most preferably from about 29 to about 34 percent; the second amine hardener (b) is from about 45 to about 60 percent; preferably from about 46 to about 56 percent; most preferably from about 49 to about 53 percent, and the third amine hardener (c) is from about 10 to about 25 percent; preferably from about 12 to about 22 percent; most preferably from about 15 to about 20 percent, all of the foregoing percentages being by weight based on the total weight of a+b+c.
  • the hardener system further includes other additives.
  • the total hardener in the system is from about 5 to about 90 percent and more narrowly from about 10 to about 70 percent. The remainder to equal 100 percent being the other additives.
  • One of these additives is a catalyst which is generally a dicarboxylic acid and is preferably salicylic acid. This is used in an amount of from about 2 to about 10, and preferably from about 3.5 to about 5.5 per parts by weight per 100 parts by weight of amine hardener system a+b+c.
  • a plasticizer which is a high boiling alcohol such as the aromatic alcohols, including for example, benzyl alcohol which has a boiling point of 401°F. This is used in an amount of from about 5 to about 25; and preferably from about 10 to about 20, most preferably 15 to 20 parts by weight per 100 parts of amine hardener system (i.e. based on the total weight of a+b+c).
  • a thixotropic agent may be used in an amount to achieve the desirable viscosity which is from about 3,000 to about 8,000, centipoises. This thixotropic agent is preferably fumed silica or silicon dioxide. It is added in an amount of from about 0.5 to 5 parts; preferably from about 1 to about 4 parts by weight per 100 parts amine hardener system (a+b+c).
  • the hardener system achieves an appropriate color depending on the application and in particular for road markers being white and yellow, a viscosity of from about 3,000 to about 20,000 centipoises, and further desirably physical properties, such as compression set and tensile elongation. It is desirable that the compressive strength is at least 5,000, and desirably from about 12,000 psi to about 14,000 psi as compressive strength as determined by ASTM D695, and the tensile strength is at least about 5,000, and more preferably at least 6000 psi as determined by ASTM D-638.
  • the urethane composition is generally a liquid at ambient temperature, for example from about 10°C to about 40°C, and preferably from about 15°C to about 30°C. It is an important aspect of the present invention that the urethane composition be volatile-free, that is generally contains less than 10 percent by weight of volatiles therein, such as a solvent, desirably less than 1 percent by weight, and preferably no volatiles at all. Such compositions are generally described as a 100 percent solids composition. Another definition of the 100 percent volatile-free urethane system is that the system, before reaction, does not contain any components which have a boiling point of less than 120°F, even though it may be liquid.
  • the urethane composition is the reaction of a two-part or component system, that is generally an intermediate component and a polyisocyanate component. Whenever it is desirable to prevent yellowing of the urethane composition, all components and compounds thereof are aliphatic.
  • the intermediate component system can be a hydroxyl terminated lactone intermediate, and/or a hydroxyl terminated polyether, polyester, or a polyether-ester intermediate.
  • the lactone based hydroxyl terminated compound can either be difunctional, trifunctional, tetrafunctional, or combinations thereof, for example, blends of a difunctional lactone based intermediate and a trifunctional based lactone intermediate, or the like.
  • a lactone intermediate can have from about 2.0 to about 4.0 or preferably to about 3.0 hydroxyl groups per molecule.
  • the hydroxyl terminated lactone intermediate is made from a lactone generally having from about 4 to about 8 carbon atoms with 6 carbons, that is caprolactone, being preferred.
  • the lactone is typically reacted with a diol generally having from 2 to 8 carbon atoms and preferably from 2 to 6 carbon atoms to form the hydroxyl terminated lactone intermediate.
  • diols include ethylene glycol, propylene glycol, butylene glycol such as 1,4-butane diol, hexamethylene glycol, and the like with 1,4-butanediol being preferred.
  • a lactone triol intermediate can be generally made from a triol having from 3 to 12 carbon atoms, desirably from 5 to 8 carbon atoms, with specific examples including glycerol, trimethylol propane, and the like.
  • a preferred triol is 2-ethyl-2-(hydroxymethyl) 1,3 propane diol, i.e., trimethylol propane.
  • various tetraols known to the art and to the literature can be utilized to make the lactone polyol intermediate.
  • the lactone-based diol or triol intermediate is a liquid at ambient temperature, it generally has a low molecular weight as from about 200 to about 1,000, and desirably from about 275 to about 450.
  • a solid lactone intermediate may be used if it is heated above its melting point, and uniformly dispersed prior to application.
  • the lactone is preferably a liquid at ambient temperature.
  • a polyol intermediate can be utilized which can either be a polyester polyol, a polyether polyol, or a polyester-ether polyol intermediate. These polyol intermediates are solvent-free.
  • the polyether intermediate is generally made from oxyalkylene compounds having from 2 to 6 carbon atoms and preferably 2 or 3 carbon atoms, i.e. specific examples include ethylene oxide, propylene oxide, butylene oxide, and the like, with ethylene oxide and propylene oxide being preferred.
  • the ester intermediate is generally made from glycols or triols having from about 2 to about 10 and desirably from about 2 to about 6 carbon atoms, with specific examples including ethylene glycol, propylene glycol, butylene glycol, hexamethylene glycol, trimethanol propane, and the like, with ethylene glycol and propylene glycol being preferred.
  • the polycarboxylic acids such as a tri- or preferably dicarboxylic acids are utilized to form the ester intermediate is an aliphatic or cycloaliphatic generally containing from about 2 to about 12 carbon atoms or aromatic acids generally containing from about 8 to about 20 carbon atoms with specific examples including succinic acid, glutaric acid, adipic acid, pimelic acid, azelaic acid, phthalic acid, diphenolic acid, and the like, with adipic acid and succinic acid being preferred.
  • a polyether polyol or a polyester polyol can be utilized, preferably a polyester-ether intermediate is utilized made from the above ester and ether forming polyol compounds and preferably a branched polyester- ether intermediate is utilized desirably having at least two hydroxyl end groups therein.
  • the mixed polyester-ether is multifunctional as containing from about 2.0 to about 3.0 hydroxyl groups therein and preferably is trifunctional.
  • An example of a highly preferred mixed polyester-ether branch polyol intermediate is Desmophen 1155 manufactured by Mobay. This intermediate has a hydroxy number of approximately 168 and an equivalent weight of 333.
  • the equivalent weight of the polyether, the polyester, or the polyether-ester intermediate is generally from about 190 to about 500 and preferably from about 300 to about 400.
  • the total amount of the various one or more polyol intermediates is generally from about 30 to about 75 parts by weight, desirably from about 40 to about 60 parts, and preferably from about 45 to about 55 parts by weight for every 100 parts by weight of the entire intermediate component.
  • the lactone based intermediate is preferred and if another polyol intermediate is utilized in association therewith, the amount thereof is up to about 50 percent; preferably up to about 10 percent; and most preferably up to about 6 percent by weight based upon the total weight of the lactone and the other (e.g. polyether polyol) intermediates.
  • the intermediate component also generally has a significant amount of one or more chain extenders which generally imparts stiffness to reacted urethane composition.
  • chain extenders can be diols, triols, etc. having from about 2 to about 15 carbon atoms and preferably from about 2 to about 6 carbon atoms with specific examples including ethylene glycol, propylene glycol, butane diol, dipropylene glycol, diethylene glycol, glycerol, trimethylol propane diol, and the like, with the diols and specifically 1,4-butane diol being preferred.
  • the amount of the chain extender is generally from about 5 to about 25 parts, and more preferably from about 10 to about 20, and most preferably from about 14 to about 16 parts by weight for every 100 parts by weight of the entire intermediate component.
  • one or more water or moisture scavengers is utilized to generally provide a moisture free composition.
  • moisture scavengers are generally known to the art as well as to the literature.
  • a particular suitable moisture scavenger has been found to be a latent aliphatic polyamine which are generally the reaction of a diisocyanate with a hydroxyl terminated oxazolidine, such as
  • R a , R b , R c , R d , and R e independently, are alkyl having from 1 to 6 carbon atoms, and the diisocyanate is R(NCO) 2 , wherein R is an aliphatic or an aromatic, or combinations thereof, generally having from about 2 to about 20 carbon atoms with specific examples including isophorone diisocyanate, hydrogenated diphenylmethane diisocyanate (HMDI), hexamethylene diisocyanate (HDI), toluene diisocyanate, and the like, but diphenylmethane diisocyanate (MDI) is generally not utilized.
  • HMDI hydrogenated diphenylmethane diisocyanate
  • HDI hexamethylene diisocyanate
  • MDI diphenylmethane diisocyanate
  • a desirable latent amine moisture scavenger is sold under the tradename HARDENER OZ by Mobay Chemical.
  • anhydride water scavengers having a total of from 4 to 12 carbon atoms, and alkaline earth salts of such anhydrides, such as methylhexahydrophthalic anhydride sold under the tradename Luketherm-M.
  • Other anhydrides include acetic anhydride, propionic anhydride, butyric anhydride, valeric anhydride, hexanoic anhydrided, pivalic anhydride, and the like.
  • molecular sieves which are generally crystalline aluminosilicates, crystalline aluminophosphates, etc. and are dispersed in a carrier oil, can be utilized.
  • a specific example is Unisiv paste sold by UOP.
  • the amount of the one or more water scavengers is generally from about 1 to about 8, and preferably from about 2 to about 6 and most preferably about 3.5 to about 4.5 parts by weight for every 100 parts by weight of the entire intermediate component.
  • the second part of the urethane composition that is the polyisocyanate component, i.e. R(NCO) n , wherein n is from 1 to about 4 and R can be an aliphatic polyisocyanate wherein R generally contains a total of from about 2 to about 20 carbon atoms and desirably from about 4 to about 10 carbon atoms.
  • Aromatic polyisocyanates that is aliphatic substituted polyisocyanates such as alkyl substituted polyisocyanates, aromatic substituted aliphatic polyisocyanates, etc. can also be utilized and R generally contains a total of from 6 to about 20 carbon atoms.
  • the polyisocyanate is desirably a diisocyanate, although optionally up to 10 percent by weight of a tri or tetraisocyanate can be utilized.
  • specific aliphatic diisocyanates include the various isophorone diisocyanates (IPDI), the various hexane diisocyanates such as 1,6-hexane diisocyanate, the various mixed trimethylhexane diisocyanates, the various pentamethylene diisocyanates, and the like. Hexamethylene diisocyanate and isophorone diisocyanate are preferred.
  • the aliphatic polyisocyanates generally have a molecular weight of from about 150 to about 600 and an equivalent weight average of from 80 to about 400.
  • aromatic diisocyanates examples include para-phenylene diisocyanate, 4,4'-dibenzyl diisocyanate, dianisidene diisocyanate, meta-phenylene diisocyanate, tolylene diisocyanate, bitolylene diisocyanate, 4,4'-methylenebisphenyl isocyanate (MDI), naphthalene diisocyanate, xylene diisocyanate, and the like with MDI being preferred.
  • MDI 4,4'-methylenebisphenyl isocyanate
  • the aromatic polyisocyanates generally have a molecular weight of from about 100 to about 700 and an equivalent weight average of from 80 to 300.
  • aromatic type diisocyanates generally give very good properties, they tend to "yellow" the urethane composition and, hence, in various situations where color or other optical properties are important, the aliphatic polyioscyanates are preferred.
  • the equivalent molecular ratio of NCO to OH of all of the various hydroxyl terminated intermediate compounds and chain extenders, etc. is generally a slight excess as from about 0.9 to about 1.5, desirably from about 1.02 to about 1.15, and preferably from about 1.05 to about 1.10. Ratios outside of this range generally yield a reacted product which is too flexible or too hard.
  • catalysts can be utilized such as dibutyl tin dilaurate, bismuth stearate, bismuth stannate, zinc octate, lead octate, cobalt naphthalates, and the like.
  • the amount of such catalyst is generally small and can range from about 0 to about 2 parts by weight and preferably from about 0.1 to about 0.6 parts by weight for every 100 parts by weight of the hydroxyl containing intermediate component.
  • the catalyst permit rapid cure at ambient temperature.
  • additives in suitable amounts can be utilized in the intermediate component.
  • additives include fillers such as clays, silicas, and the like, various antioxidants, various ultraviolet light inhibitors, air release agents, leveling agents, wetting agents, and the like, as well as pigments.
  • the pigments utilized are generally titanium dioxide for white, and lead chromate and various organic pigments for yellow. Of course other pigments can be utilized.
  • the epoxy composition and the urethane composition of the present invention are generally utilized as a laminate or layer system to form an article having good binding strength to the substrate and yet good abrasion resistance and weatherability resistance which is supplied by the urethane composition.
  • the articles or laminates of the present invention can be utilized as protective coatings for concrete floors, steel structures, storage tanks, including tanks containing corrosive material, road lane markers, and the like. These structures can be formed of various substrate materials including, for example, steel concrete and asphalt. Since the epoxy composition has good bonding strength, it is generally utilized as a base or substrate interface layer.
  • the two-part epoxy system is applied by mixing both parts together in any conventional manner and applying the same to the surface to be treated or coated in any conventional manner as by brushing, spraying, and the like.
  • the thickness of the epoxy base layer will vary depending upon the surface being coated and also upon the desired degree of protection sought.
  • the thickness of the epoxy base layer which is applied is generally from about 5 to about 20 mils, desirably from about 8 to about 15 mils and preferably from about 10 to about 12 mils.
  • the generally liquid, twopart epoxy system can be contained on a vehicle in separate tanks, subsequently mixed under high pressure and immediately thereafter applied to an appropriate position of a road to indicate a lane marker thereon. Upon a mixing of the generally liquid solvent-free two part epoxy component system, reaction immediately commences at ambient temperature.
  • Application to the road or other substrate can be in any conventional manner as by brushing, spraying, and the like.
  • the two-part solvent free, generally liquid, urethane system which can be stored in separate containers is mixed in any convention manner, and generally applied under pressure to the top of the previously applied epoxy composition. Upon mixing, the two-part urethane system will immediately commence reaction and hence it is immediately applied to the base layer before any substantial crosslinking or curing reaction occurs. Application can be in any conventional manner as by brushing, spraying, and the like.
  • the thickness of the urethane layer will depend upon the surface being treated and the degree of protection sought and with regard to road lane marker, the urethane is generally applied at a thickness of from about 0.5 to about 10 mils, desirably from about 0.75 to about 5 mils, and preferably 2 or 3 mils.
  • the urethane composition must be applied while the epoxy base layer is still tacky and may be cured while the epoxy system is still curing.
  • the two-part urethane composition can be applied by a second vehicle following the first vehicle.
  • the urethane composition can be contained on the same vehicle which first applies the epoxy base and shortly thereafter applies the urethane composition.
  • the two-part urethane composition When the two-part urethane composition is applied to a non-fully cured epoxy coating or base layer, there might will be some bleeding or co-mingling of the urethane composition into the epoxy composition. It is desired that the epoxy base layer is not fully cured when the urethane is applied so that a chemical bond will form between the layers. Because of the ingredients of both the epoxy system and the urethane system cure occurs at ambient temperatures.
  • the article or laminate is utilized as a road lane marker
  • nighttime reflectivity is obtained by adding transparent spheres to laminate, such as ceramic spheres and preferably glass spheres.
  • the method of application generally involves simply sprinkling the spheres on the urethane layer while the same is still wet, i.e. not fully cured.
  • the size of the various spheres will vary according to the application. Glass spheres are preferred and are readily available and generally contain a conventional sizing thereon as for example an amino silane.
  • the present invention achieves good adhesion of the spheres as well as achieving good adhesion to the substrate.
  • the particular laminate or article of the present invention when utilized as a lane marker results in excellent adhesion to the road surface and yet offers excellent weatherability and abrasion resistance and is expected to yield an article having a long term life.
  • the glass beads have been found to have excellent adhesion to the epoxy urethane laminate.
  • Bisphenol A diglycidyl ether polymer (Araldite 6010), and butyl glycidyl ether (CWC-61) were mixed for eight minutes. Titanium dioxide (Ti-pure 960) and the amorphous fumed silica were added at high speed for 15- 20 minutes to the above mixture. The defoamer was added and the mixture was blended at slow speed for three to four minutes.
  • Silicon-di-oxide 41.0 The three amines (Ancamine ® 1644, sold by
  • Example 2 The tensile strength as measured by ASTM D638 was 6,000, the abrasion resistance as measured by ASTM C501 was about 65 mgs. The ultra violet stability as measured by ASTM-G53 was good. Shore D hardness was between about 70 and about 80 as measured by ASTM D2260 and the compressive strength as measured by ASTM D695 was more than 12,000 psi. Example 2
  • a laboratory scale sample was made in process similar to that set forth in Example 1, excep that an epoxide fraction in the range of C 8 to C 10 (i.e.
  • Heloxy 7, sold by Rhone-Poulenc was used as a diluen rather than butyl glycidyl either. Further, the defoamer was omitted.
  • a one component amine hardener was used which was an aliphatic amine (i.e. Versamine 900, sold by Henkel). The specific formulation and the results are set forth in Table IV.
  • a laboratory scale sample was made in a process similar to that set forth in Example 1 except that a urethane acrylate modifier was used which was Ancarez 300A, sold by Pacific Anchor. This was used with a two-component amine hardener system which was amino-ethyl-piperazine and nonylphenol and a modified cycloaliphatic (Ancamine 1895, sold by Pacific Anchor) .
  • the specific formulation and resulsts are set forth in Table VI. TABLE VI
  • a laboratory scale sample was made in a process similar to that set forth in Example 2 using a three-component amine hardener system comprising diethylenetriethyleneamine with bisphenol A (Versamine 912, sold by Henkel), dimethylenetriamine (DETA-HP, sold by Pacific Anchor), and aliphatic amine (Versamine 711, sold by Henkel).
  • the specific formulation and results are set forth in Table VII. TABLE VII
  • Example 1 A laboratory scale sample was made as set forth generally in Example 1 using silicon dioxide and amorphous fumed silica. The formulation was combined with a one-component mercaptan hardener, a mercaptan terminated polysulfide (Capcure 3-800, sold by Henke), and a trisubstituted phenol accelerator (Capcure EH-30, sold by Henkel), was also used. The specific formulation and results are set forth in Table VIII. TABLE VIII
  • polyesterether polyol (Desmophen 1155) (15.6 lbs.) and 1,4-butanediol (43.5 lbs.). The mixture was stirred at room temperature for 3-4 minutes. To the mixture was then added titanium dioxide (69.6 lbs.) and stirred at room temperature for five minutes.
  • the mixture from above was reacted with one equivalent of polymeric 1,6-hexamethylenediisocynate (Demodur N3200).
  • the gel time for 100 gms. mixed material was 3 minutes at 25°C and the following physical properties were observed after 7 day cure: tensile strength - 3,000 psi (ASTM D638), abrasion resistance ⁇ 10 mg (ASTM C501) and Shore D 78 (ASTM D2260).
  • the mixture from above was reacted with one equivalent of polymeric 1,6-hexamethylenediisocyanate (Demodur N3200).
  • the gel time for 100 gms. mixed material was 2-1/2-3 minutes at 25°C and the following physical properties were observed after seven day cure: tensile strength 4,000 psi (ASTM D638), abrasion resistance ⁇ 20 mg (ASTM C501) and Shore D 80 (ASTM D2260).
  • Example 7 Same as for Example 7, but 1.1 lbs. of dibutyltindilaurate was used. The resulting mixture was reacted with one equivalent of polymeric, 1,6-hexamethylenediisocyanate (Desmodur N3200). The gel time for 100 gms. mixed material was 2-2.25 mins. at 25°C and the following physical properties were observed after seven day cure: tensile strength 2,600 psi (ASTM D638), abrasion resistance ⁇ 20 mg. (ASTM C501) and Shore D 79 (ASTM D2260).
  • ASTM D638 tensile strength 2,600 psi
  • ASTM C501 abrasion resistance ⁇ 20 mg.
  • Shore D 79 ASTM D2260
  • Example 8 Same as for Example 8, but 0.54 lbs. of dibutylditindilaurate was used. The resulting mixture was reacted with one equivalent of polymeric 1,6-hexamethylenediisocyanate (Desmodur N3200). The gel time for 100 gms. mixed material was 4-1/2-5 mins. at 25°C and the following physical properties were observed after seven day cure: tensile strength 3,600 psi (ASTM D638), abrasion resistance ⁇ 40 mg. (ASTM C501) and Shore D 80 (ASTM D2260).
  • tensile strength 3,600 psi ASTM D638
  • ASTM C501 abrasion resistance ⁇ 40 mg.
  • Shore D 80 ASTM D2260
  • the mixture from above was reacted with polymeric diphenylmethane diisocyanate (Mondur MRS, 290.3 lbs).
  • the gel time for 100 gms mixed material was 4-5 minutes at 25°C and the following physical properties were observed after seven day cure: tensile strength 2600 psi (ASTM D 638), abrasion resistance ⁇ 60 mg (ASTM C501) and Shore D 80 (ASTM D2260).
  • the mixture from above was reacted with polymeric diphenylmethane diisocyanate (Mondur MRS, 162.6 lbs).
  • the gel time for 100 gms mixed material was 5 minutes at 25°C and the following physical properties were observed after seven day cure: tensile strength 2900 psi (ASTM D638), abrasion resistance ⁇ 65 mg (ASTM C501) and Shore D 75 (ASTM D2260).
  • the mixture from above was reacted with 45.9 lbs of polymeric 1,6-hexamethylene diisocyanate Desmodur N3200.
  • the gel time for 100 gms mixed material was 5 minutes at 25°C and the following physical properties were observed after seven day cure: tensile strength 2600 psi (ASTM D 638), abrasion resistance ⁇ 20 mg (ASTM C501) and Shore D 70.
  • Example 1 An epoxy coating as described in Example 1 was cured with hardener described in Example 1 and applied at thickness of 12 mils. Immediately on top was placed a polyurethane coating prepared as described in Example 7. The polyurethane coating was applied at a thickness of 3-4 mils. The composite coating was cured for 3 days at room temperature and then found to give the following properties: Abrasion resistance ⁇ 10 mg (ASTM C501); adhesion to concrete: failure in concrete (ACI 503); weathering resistance: no change in color after 750 hours, 4 hours humidity, 50°C, 4 hours UV (ASTM-G53). The test was stopped prior to discoloration.
  • Example 15 Essentially prepared as Example 15, but after the polyurethane coating had been applied glass beads were also applied. After 3-day cure at room temperature, the composite was found to show no change in color when subjected to accelerated weathering as described in Example 15.
  • Example 5 To an industrial concrete floor was applied an epoxy coating prepared as described in Example 5 at a thickness of 5 mils. Just prior to the epoxy coating becoming tack free, a polyurethane coating prepared as described in Example 13 was applied on it at a thickness of approximately 10 mils.
  • the flooring system was allowed to cure at 25°C for 12 hours and the floor returned to its normal use.
  • the floor system was found to be aesthetically pleasing, self-leveled, easy to maintain with excellent abrasion, and impact properties as well as good chemical resistance.
  • the present invention has no volatile organic components.
  • the organic structure when based on aliphatic compositions rather than aromatic compositions has superior weatherability and resistance to discoloration.
  • the intermediate isocyanate chemistry results in a urethane which is flexible and yet tough to very rigid by varying the chain length of either the intermediate or the isocyanate prepolymers or monomers.
  • the resulting composition has excellent physical properties for the intended use as well good chemical properties.
  • the method of application results in a permanent chemical fusion between the layers.
  • the epoxy layer has good wetability, while the urethane layer allows for a short tack free time.
  • the short tack free time limits the amount of time that dirt can make it onto the surface, and shortens the time before cars can drive on the surface.
  • the chemical fusion between the layers can be understood as the chemical reaction between the two layers which becomes a part of the polymeric structure having no discrete interface, but a form of crosslinking between the layers. It is possible to drive over the present composition within 5 to 10 minutes without harming the composition, whereas in contrast, in the past it has been necessary to wait a cure time of 60 to 75 minutes.

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Abstract

L'article obtenu comprend un revêtement de base époxyde et une couche supérieure d'uréthane utile dans des applications de marquage des chaussées. La composition époxyde est un système bicomposé, entièrement exempt d'agents volatils et contenant un ou plusieurs agents de durcissement qui réagissent avec un composant époxy tel que l'éther glycidyle de bisphénole A. La composition d'uréthane est également un système bicomposé entièrement exempt d'agents volatils et contenant un composant polyisocyanate et un composant intermédiaire comprenant un polyol de polylactone et/ou un polyol de polyéther, un polyol de polyester ou un polyol de polyéther-ester, un agent d'allongement à chaîne polyol aliphatique et un agent adsorbant l'humidité. La composition époxyde à deux composants peut être appliquée sur une route avec une couche de revêtement de la composition uréthane afin de réaliser des lignes de marquage des voies de circulation routière. La composition uréthane est résistante aux éléments et à l'abrasion ainsi qu'au jaunissement. Divers composés réfléchissants tels que des billes de verre peuvent être appliqués ou partiellement noyés dans la composition pour lui conférer un pouvoir réfléchissant de nuit ainsi que de nuit et par temps pluvieux.
PCT/US1992/009941 1991-11-14 1992-11-12 Compositions de revetement contenant des composants urethanes et epoxy, et articles revetus de ces compositions WO1993010167A1 (fr)

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SG83824A1 (en) * 1999-11-25 2001-10-16 Rohm & Haas Method for producing fast drying multi-component waterborne coating compositions
US6607831B2 (en) 2000-12-28 2003-08-19 3M Innovative Properties Company Multi-layer article
US6709748B1 (en) 1998-04-22 2004-03-23 3M Innovative Properties Company Flexible polyurethane material
WO2010036522A1 (fr) * 2008-09-25 2010-04-01 Dow Global Technologies Inc. Marqueurs de voies routières réfléchissants résistants à l'usure et aux impacts

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Publication number Publication date
DE69224480D1 (de) 1998-03-26
EP0603342B1 (fr) 1998-02-18
DE69224480T2 (de) 1998-08-06
EP0603342A1 (fr) 1994-06-29
CA2106204A1 (fr) 1993-05-15
US5340652A (en) 1994-08-23
EP0603342A4 (fr) 1994-12-14

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